Cargando…

Neuroimaging Biomarkers Predict Brain Structural Connectivity Change in a Mouse Model of Vascular Cognitive Impairment

BACKGROUND AND PURPOSE—: Chronic hypoperfusion in the mouse brain has been suggested to mimic aspects of vascular cognitive impairment, such as white matter damage. Although this model has attracted attention, our group has struggled to generate a reliable cognitive and pathological phenotype. This...

Descripción completa

Detalles Bibliográficos
Autores principales: Boehm-Sturm, Philipp, Füchtemeier, Martina, Foddis, Marco, Mueller, Susanne, Trueman, Rebecca C., Zille, Marietta, Rinnenthal, Jan Leo, Kypraios, Theodore, Shaw, Laurence, Dirnagl, Ulrich, Farr, Tracy D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5266417/
https://www.ncbi.nlm.nih.gov/pubmed/28070001
http://dx.doi.org/10.1161/STROKEAHA.116.014394
_version_ 1782500467308232704
author Boehm-Sturm, Philipp
Füchtemeier, Martina
Foddis, Marco
Mueller, Susanne
Trueman, Rebecca C.
Zille, Marietta
Rinnenthal, Jan Leo
Kypraios, Theodore
Shaw, Laurence
Dirnagl, Ulrich
Farr, Tracy D.
author_facet Boehm-Sturm, Philipp
Füchtemeier, Martina
Foddis, Marco
Mueller, Susanne
Trueman, Rebecca C.
Zille, Marietta
Rinnenthal, Jan Leo
Kypraios, Theodore
Shaw, Laurence
Dirnagl, Ulrich
Farr, Tracy D.
author_sort Boehm-Sturm, Philipp
collection PubMed
description BACKGROUND AND PURPOSE—: Chronic hypoperfusion in the mouse brain has been suggested to mimic aspects of vascular cognitive impairment, such as white matter damage. Although this model has attracted attention, our group has struggled to generate a reliable cognitive and pathological phenotype. This study aimed to identify neuroimaging biomarkers of brain pathology in aged, more severely hypoperfused mice. METHODS—: We used magnetic resonance imaging to characterize brain degeneration in mice hypoperfused by refining the surgical procedure to use the smallest reported diameter microcoils (160 μm). RESULTS—: Acute cerebral blood flow decreases were observed in the hypoperfused group that recovered over 1 month and coincided with arterial remodeling. Increasing hypoperfusion resulted in a reduction in spatial learning abilities in the water maze that has not been previously reported. We were unable to observe severe white matter damage with histology, but a novel approach to analyze diffusion tensor imaging data, graph theory, revealed substantial reorganization of the hypoperfused brain network. A logistic regression model from the data revealed that 3 network parameters were particularly efficient at predicting group membership (global and local efficiency and degrees), and clustering coefficient was correlated with performance in the water maze. CONCLUSIONS—: Overall, these findings suggest that, despite the autoregulatory abilities of the mouse brain to compensate for a sudden decrease in blood flow, there is evidence of change in the brain networks that can be used as neuroimaging biomarkers to predict outcome.
format Online
Article
Text
id pubmed-5266417
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Lippincott Williams & Wilkins
record_format MEDLINE/PubMed
spelling pubmed-52664172017-02-08 Neuroimaging Biomarkers Predict Brain Structural Connectivity Change in a Mouse Model of Vascular Cognitive Impairment Boehm-Sturm, Philipp Füchtemeier, Martina Foddis, Marco Mueller, Susanne Trueman, Rebecca C. Zille, Marietta Rinnenthal, Jan Leo Kypraios, Theodore Shaw, Laurence Dirnagl, Ulrich Farr, Tracy D. Stroke Original Contributions BACKGROUND AND PURPOSE—: Chronic hypoperfusion in the mouse brain has been suggested to mimic aspects of vascular cognitive impairment, such as white matter damage. Although this model has attracted attention, our group has struggled to generate a reliable cognitive and pathological phenotype. This study aimed to identify neuroimaging biomarkers of brain pathology in aged, more severely hypoperfused mice. METHODS—: We used magnetic resonance imaging to characterize brain degeneration in mice hypoperfused by refining the surgical procedure to use the smallest reported diameter microcoils (160 μm). RESULTS—: Acute cerebral blood flow decreases were observed in the hypoperfused group that recovered over 1 month and coincided with arterial remodeling. Increasing hypoperfusion resulted in a reduction in spatial learning abilities in the water maze that has not been previously reported. We were unable to observe severe white matter damage with histology, but a novel approach to analyze diffusion tensor imaging data, graph theory, revealed substantial reorganization of the hypoperfused brain network. A logistic regression model from the data revealed that 3 network parameters were particularly efficient at predicting group membership (global and local efficiency and degrees), and clustering coefficient was correlated with performance in the water maze. CONCLUSIONS—: Overall, these findings suggest that, despite the autoregulatory abilities of the mouse brain to compensate for a sudden decrease in blood flow, there is evidence of change in the brain networks that can be used as neuroimaging biomarkers to predict outcome. Lippincott Williams & Wilkins 2017-02 2017-01-23 /pmc/articles/PMC5266417/ /pubmed/28070001 http://dx.doi.org/10.1161/STROKEAHA.116.014394 Text en © 2017 The Authors. Stroke is published on behalf of the American Heart Association, Inc., by Wolters Kluwer Health, Inc. This is an open access article under the terms of the Creative Commons Attribution Non-Commercial-NoDervis (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited, the use is noncommercial, and no modifications or adaptations are made.
spellingShingle Original Contributions
Boehm-Sturm, Philipp
Füchtemeier, Martina
Foddis, Marco
Mueller, Susanne
Trueman, Rebecca C.
Zille, Marietta
Rinnenthal, Jan Leo
Kypraios, Theodore
Shaw, Laurence
Dirnagl, Ulrich
Farr, Tracy D.
Neuroimaging Biomarkers Predict Brain Structural Connectivity Change in a Mouse Model of Vascular Cognitive Impairment
title Neuroimaging Biomarkers Predict Brain Structural Connectivity Change in a Mouse Model of Vascular Cognitive Impairment
title_full Neuroimaging Biomarkers Predict Brain Structural Connectivity Change in a Mouse Model of Vascular Cognitive Impairment
title_fullStr Neuroimaging Biomarkers Predict Brain Structural Connectivity Change in a Mouse Model of Vascular Cognitive Impairment
title_full_unstemmed Neuroimaging Biomarkers Predict Brain Structural Connectivity Change in a Mouse Model of Vascular Cognitive Impairment
title_short Neuroimaging Biomarkers Predict Brain Structural Connectivity Change in a Mouse Model of Vascular Cognitive Impairment
title_sort neuroimaging biomarkers predict brain structural connectivity change in a mouse model of vascular cognitive impairment
topic Original Contributions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5266417/
https://www.ncbi.nlm.nih.gov/pubmed/28070001
http://dx.doi.org/10.1161/STROKEAHA.116.014394
work_keys_str_mv AT boehmsturmphilipp neuroimagingbiomarkerspredictbrainstructuralconnectivitychangeinamousemodelofvascularcognitiveimpairment
AT fuchtemeiermartina neuroimagingbiomarkerspredictbrainstructuralconnectivitychangeinamousemodelofvascularcognitiveimpairment
AT foddismarco neuroimagingbiomarkerspredictbrainstructuralconnectivitychangeinamousemodelofvascularcognitiveimpairment
AT muellersusanne neuroimagingbiomarkerspredictbrainstructuralconnectivitychangeinamousemodelofvascularcognitiveimpairment
AT truemanrebeccac neuroimagingbiomarkerspredictbrainstructuralconnectivitychangeinamousemodelofvascularcognitiveimpairment
AT zillemarietta neuroimagingbiomarkerspredictbrainstructuralconnectivitychangeinamousemodelofvascularcognitiveimpairment
AT rinnenthaljanleo neuroimagingbiomarkerspredictbrainstructuralconnectivitychangeinamousemodelofvascularcognitiveimpairment
AT kypraiostheodore neuroimagingbiomarkerspredictbrainstructuralconnectivitychangeinamousemodelofvascularcognitiveimpairment
AT shawlaurence neuroimagingbiomarkerspredictbrainstructuralconnectivitychangeinamousemodelofvascularcognitiveimpairment
AT dirnaglulrich neuroimagingbiomarkerspredictbrainstructuralconnectivitychangeinamousemodelofvascularcognitiveimpairment
AT farrtracyd neuroimagingbiomarkerspredictbrainstructuralconnectivitychangeinamousemodelofvascularcognitiveimpairment